Diagnosis Code: Q04.2

Short Description: Holoprosencephaly

Long Description: Holoprosencephaly

The code Q04.2 is VALID for claim submission

Code Classification:

• Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
  • Congenital malformations of the nervous system (Q00-Q07)
    • Other congenital malformations of brain (Q04)
      • Q04.2 Holoprosencephaly

Code Version: 2022 ICD-10-CM

Synonyms

• Agenesis of pancreas
• Agnathia, holoprosencephaly, situs inversus syndrome
• Alobar holoprosencephaly
• Cebocephaly
• Congenital absence of pancreas
• Congenital stenosis of nasal pyriform aperture
• Hartsfield syndrome
• Holoprosencephaly and postaxial polydactyly syndrome
• Holoprosencephaly craniosynostosis syndrome
• Holoprosencephaly sequence
• Holoprosencephaly with caudal dysgenesis syndrome
• Holoprosencephaly with nasal pyriformis aperture
• Kundrat's syndrome
• Lobar holoprosencephaly
• Microform holoprosencephaly
• Middle interhemispheric variant of holoprosencephaly
• Morse Rawnsley Sargent syndrome
• Pancreatic agenesis, holoprosencephaly syndrome
• Semi-lobar holoprosencephaly

Crosswalk Information

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This page was last updated on: 10/1/2023

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